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Develop technical and financial analyses to support regulatory case filings and strategies related to customer programs (including but not limited to Demand Side Management (DSM), Demand Response (DR), and other customer programs). Serve as subject matter experts on regulated customer programs in resource planning, rate case, and other processes. Communicate and work effe
Posted Today
Stirling Q&R Ltd
- Minneapolis, MN
Prepare and submit regulatory filings to FDA and MHRA (UK) Maintain current knowledge of US and EU guidelines and legislation relating to medical device regulation Oversee all aspects of premarket approval applications and post market surveillance programs Ensure regulatory compliance with all applicable laws, statutes, rules, regulations, and guidances pertaining to medi
Posted 1 day ago
Saluda Medical
- Minneapolis, MN
Salary At Saluda, we challenge boundaries. We innovate and think beyond the conventional. We disrupt. With the passion and energy of an accomplished team of seasoned experts, our focus is to revolutionize the standard of care in the neuromodulation space by transforming the lives of patients suffering from debilitating pain. Saluda is a global healthcare company that is r
Posted 1 day ago
Inspire Medical Systems I
- Minneapolis, MN
We are recruiting for an International Regulatory Affairs Manager to join our team located in the Minneapolis, MN location. Reporting directly into the Vice President of Regulatory Affairs, you will be responsible for establishing strategy and supporting execution of global regulatory activities to obtain and maintain regulatory approvals in countries outside the United S
Posted 1 day ago
Stirling Q&R Ltd
- Minneapolis, MN
Ensure medical device compliance with FDA regulations and applicable ISO standards Review the technical documentation for completeness, accuracy, adherence to regulatory requirements, and completeness of information provided Provide input to design specifications, engineering drawings and other documents Develop test plans and procedures Perform inspections and audits of
Posted 1 day ago
Under minimal supervision, the Senior Regulatory Affairs Specialist is responsible for planning, managing, and implementing regulatory approvals to the FDA, notified body and other country specific product registrations. The position is also responsible for ensuring continued compliance with regulatory agency approvals. Key Responsibilities Develops domestic and internati
Posted 1 day ago
The Principal Regulatory Affairs Specialist is responsible for design control compliance for assigned products and will develop and execute regulatory strategies per time lines to assure clearance/approval in the assigned geographies. This position will also prepare, monitor, and communicate status of regulatory submissions and perform duties related to regulatory affairs
Posted 2 days ago
The U.S. Regulatory Manager, is responsible for all Zinpro's U.S. regulatory projects, leading and advising on regulatory requirements and route to market for newly developed products. This includes management of external regulatory consultants in U.S. as well as interaction with respective national, regional, and international regulatory authorities and industry associat
Posted 2 days ago
A Data Governance Program Manager is part of the Enterprise Digital Intelligence (Edi) team and is responsible for leading & coordinating the development and on going adoption of our data governance framework. This role requires knowledge of governance policies, master data requirements, and both business & technical understanding of data and usage. The Data Governance Pr
Posted 2 days ago
These examples do not include all possible tasks in this work and do not limit the assignment of related tasks in any position of this classification. Regular attendance according to the position's management approved work schedule is required for all positions. 1. Perform, direct, and coordinate property research with other County departments and Title and Abstract compa
Posted 5 days ago
The Senior Material Handler is a functional role that includes material handling and inventory control tasks to ensure all inventory is received, maintained accurately, and provided as required to internal customers using various indicators or signals. To assure team continuity across all warehouse operations, this position may also be required to learn, perform, and or b
Posted 8 days ago
Quidel's mission is to provide patients with immediate and frequent access to highly accurate, affordable testing for the good of our families, our communities and the world. We are a leading manufacturer of point of care diagnostic solutions. Quidel's comprehensive product portfolio includes tests for a wide range of infectious diseases, cardiac and autoimmune biomarkers
Posted 15 days ago
Answer and respond to incoming calls received in the dispatch communications center and dispatch units including police, fire, ambulance and other emergency personnel to emergency and non emergency situations. Actively listen and ask appropriate questions of callers to effectively prioritize the call and determine the necessary response. Provide ongoing updates to respond
Posted 15 days ago
Pfizer
- Tampa, FL / Milwaukee, WI / Middleton, WI / 61 more...
Pfizer Architecture and Digital Innovation Lab organization is responsible for translating the Pfizer Strategy into innovative products and digital, data, and technology business solutions for our customers, partners, and colleagues. The team leads the strategic efforts in creating an enterprise architecture and master plan that ties together our experiences, data, workfl
Posted 16 days ago
Responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process and sustaining engineering projects. Key Responsibilities Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross functional teams. Acts as company representative, developing and maintaining posit
Posted 21 days ago
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